58 phenotypes from 8 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fgf3M1Btlr/Fgf3M1Btlr C57BL/6J-Fgf3M1Btlr	curly tail	J:267538
	decreased body weight	J:267538
	kinked tail	J:267538
Fgf3tm1.1Sms/Fgf3tm1.1Sms involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ	abnormal ear morphology	J:160254
	abnormal embryo development	J:160254
Fgf3tm1.1Sms/Fgf3tm1.1Sms involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal membranous labyrinth morphology	J:128377
	abnormal scala vestibuli morphology	J:128377
	abnormal utricle morphology	J:128377
	abnormal vestibular saccule morphology	J:128377
	absent common crus	J:128377
	absent endolymphatic sac	J:128377
	absent posterior semicircular canal	J:128377
	absent superior semicircular canal	J:128377
	circling	J:128377
	curly tail	J:128377
	decreased cochlea coiling	J:128377
	dilated cochlea	J:128377
	dilated scala media	J:128377
	head tilt	J:128377
	increased or absent threshold for auditory brainstem response	J:128377
	postnatal lethality	J:128377
	short endolymphatic duct	J:128377
	short tail	J:128377
Fgf3tm1.2Sms/Fgf3tm1.2Sms involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	no abnormal phenotype detected	J:160254
Fgf3tm1Mrc/Fgf3tm1.1Sms involves: 129S1/Sv * 129S4/SvJaeSor * 129S7/SvEvBrd * 129X1/SvJ * BALB/cJ	abnormal ear morphology	J:160254
	abnormal embryo development	J:160254
Fgf3tm1Mrc/Fgf3tm1Mrc involves: 129S7/SvEvBrd	abnormal otic vesicle development	J:83659
Fgf3tm1Mrc/Fgf3tm1Mrc involves: 129S7/SvEvBrd * C57BL/6	abnormal caudal vertebrae morphology	J:4501
	abnormal cochlea morphology	J:4501
	abnormal inner ear morphology	J:4501
	abnormal inner ear vestibule morphology	J:4501
	abnormal membranous labyrinth morphology	J:4501, J:128377
	abnormal neural tube morphology	J:4501
	abnormal scala media morphology	J:4501
	abnormal semicircular canal morphology	J:4501
	abnormal somite development	J:4501
	abnormal utricle morphology	J:128377
	abnormal vestibular saccule morphology	J:128377
	abnormal vestibulocochlear ganglion morphology	J:4501
	absent common crus	J:128377
	absent endolymphatic duct	J:4501
	absent endolymphatic sac	J:4501, J:128377
	absent pinna reflex	J:4501
	absent posterior semicircular canal	J:4501, J:128377
	absent superior semicircular canal	J:128377
	caudal vertebral fusion	J:4501
	circling	J:4501
	cochlear ganglion hypoplasia	J:4501
	curly tail	J:4501, J:128377
	decreased caudal vertebrae number	J:4501
	decreased cochlea coiling	J:128377
	decreased embryo size	J:4501
	decreased startle reflex	J:4501
	dilated scala media	J:128377
	embryonic growth retardation	J:4501
	head tilt	J:4501
	hyperactivity	J:4501
	impaired righting response	J:4501
	kinked tail	J:4501
	neonatal lethality, incomplete penetrance	J:4501
	postnatal lethality, incomplete penetrance	J:4501, J:128377
	short endolymphatic duct	J:128377
	short tail	J:4501, J:128377
Fgf3tm1Sng/Fgf3tm1Sng involves: 129P2/OlaHsd * C57BL/6	abnormal tail morphology	J:87221
	normal behavior/neurological phenotype	J:87221
	normal hearing/vestibular/ear phenotype	J:87221
	normal mortality/aging	J:87221
	normal reproductive system phenotype	J:87221
	short tail	J:87221
	small otic vesicle	J:87221
	thick tail	J:87221
Fgf3tm2.1Sms/Fgf3tm2.1Sms involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	kinked tail	J:160254
Fgf3tm2Mrc/Fgf3tm2Mrc involves: 129S7/SvEvBrd * C57BL/6	abnormal caudal vertebrae morphology	J:4501
	abnormal cranial ganglia morphology	J:4501
	abnormal inner ear morphology	J:4501
	curly tail	J:4501
	decreased embryo size	J:4501
	kinked tail	J:4501
	postnatal lethality	J:4501
	short tail	J:4501
Fgf3tm4b(EUCOMM)Hmgu/Fgf3+ C57BL/6N-Fgf3tm4b(EUCOMM)Hmgu/Bay	enlarged lymph nodes	J:211773
	unresponsive to tactile stimuli	J:211773
Fgf3tm4b(EUCOMM)Hmgu/Fgf3tm4b(EUCOMM)Hmgu C57BL/6N-Fgf3tm4b(EUCOMM)Hmgu/Bay	abnormal embryo size	J:211773
	abnormal tail morphology	J:211773
	no spontaneous movement	J:211773
	preweaning lethality, complete penetrance	J:211773
	unresponsive to tactile stimuli	J:211773